- Clinical Experience
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- Dosing & Administration
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The Acthar Gel Commercial Starter Program provides Acthar Gel at no cost for a limited period of time (up to 18 months) to eligible, commercially-insured patients who have a valid prescription for Acthar® Gel for an FDA-approved indication of infantile spasms, systemic lupus erythematosus, dermatomyositis/polymyositis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, symptomatic sarcoidosis, ocular inflammatory diseases, or proteinuria in nephrotic syndrome, where there is a delay in determining whether commercial prescription coverage is available or where there is a temporary lapse in coverage. The Program is available only to patients who are residents of the United States or Puerto Rico.
The Program is not available to patients whose prescription claims are reimbursed, in whole or in part, by any state or federal government program, including, but not limited to, Medicaid, Medicare, Medigap, Department of Defense (DoD), Veterans Affairs (VA), TRICARE, Puerto Rico Government insurance, or any other government-funded health plan. The Program is not available to patients who are uninsured or who are not pursuing commercial insurance coverage for Acthar Gel, or where prohibited by law.
Eligible patients must have verified commercial insurance. Patients may be asked to reverify insurance coverage status during the course of the Program.
Enrolled patients will receive one vial of Acthar Gel at a time for up to 18 months, or until a final coverage determination is made, whichever occurs first. To remain eligible for the Program, appeal of any prior authorization denial must be made within 60 days following the date of first shipment of Acthar Gel to the enrolled patient under this Program, or within 90 days if an extension is requested. Other limitations may apply
Patients agree not to seek reimbursement from any third-party payer for all or any part of Acthar Gel dispensed pursuant to this Program. No purchase necessary. The program is not health insurance, nor is participation a guarantee of insurance coverage. Mallinckrodt reserves the right to rescind, revoke, or amend this Program at any time without notice.
By participating in the Program, the patient agrees to these terms and conditions.
Eligible patients for this Program must meet the following criteria: have proteinuria with either recurrent or de novo post-transplant FSGS that did not respond adequately to conventional therapy, or have been diagnosed with acute exacerbations of multiple sclerosis, determined by a healthcare provider to be appropriate for Acthar Gel treatment, have not used Acthar Gel (currently or in the past), must be 18 years or older, and have commercial or private insurance, and are not participating in Medicare, Medicaid, or any government-funded healthcare plan.
Eligible healthcare providers for this Program are those who are licensed practitioners qualified to request, receive, prescribe, and dispense prescription samples, have facilities to store Acthar Gel according to its label (between 2° C and 8° C or 36° F and 46° F), and will sign and return the Acknowledgment of Content (AOC) to confirm receipt of Acthar Gel samples or acknowledge in writing that a pharmacy may sign on the healthcare provider's behalf.
Eligible healthcare providers may have only 1 sample vial at a time, but up to 14 vials over the term of this Program. Eligible patients should only receive one (1) sample vial. Sample vials are not for sale, resale, trade, barter, donation, or return for credit, and sample vials received through this Program may not be billed to any third-party payer. The vials will be clearly labeled that they are not for sale.
Acthar Gel is indicated for:
Contraindications
Acthar is contraindicated:
Warnings and Precautions
Adverse Reactions
Pregnancy
Please see full Prescribing Information for additional Important Safety Information.
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